LDRT and Chemoimmunotherapy in NPC With Liver Metastasis

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-70
SponsorHunan Cancer Hospital

About this trial

This study aims to evaluate the efficacy and toxicity of adding low-dose radiotherapy to chemoimmunotherapy as a first-line treatment for nasopharyngeal carcinoma patients with liver metastasis.

Eligibility criteria

Qualifiers

Age ≥ 18 years and ≤ 70 years, male or non-pregnant female.

Histologically confirmed with nonkeratinizing carcinoma of the nasopharynx (differentiated or undifferentiated type, WHO II or III)

Stage IVB (AJCC 8th edition staging)

De novo nasopharyngeal carcinoma with liver metastasis, or patients who had received curative treatment (radical radiotherapy or radical radiotherapy combined with chemotherapy) and developed liver metastasis more than 6 months after treatment completion.

Disqualifiers

Patients with tumor recurrence at the primary site who have previously received radical radiotherapy.

Tumor invasion involving major blood vessels, with a high risk of significant bleeding as assessed by the investigator.

Systemic anticancer therapy, including hormone therapy, administered within 28 days prior to the initiation of the study treatment.

Previous treatment with immune checkpoint inhibitors (e.g., PD-1/PD-L1, CTLA-4).

Trial design

Treatments tested in this trial

  • Low-dose radiotherapy combine with chemoimmunotherapy

Treatment groups

26 Participants
are divided into 1 treatment group

Sponsors and collaborators